8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
FEKAL CHECK PARASITOLOGY CONTROL SLIDE
FDA 510(k)
FDA Class 1
·Microbiology
HEM-O-LOK LIGATION CLIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VenaCure EVLT NeverTouch Procedure Kit
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MONACO RTP SYSTEM
FDA Adverse Event
Malfunction
·IMPAC MEDICAL SYSTEMS, INC·Product code MUJ·February 20, 2014
CONCERTO CRT-D DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·October 9, 2010
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 10, 2012
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021
OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·October 13, 2021